Tsung‐Jen Liao Source Confirmed
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Researcher
National Center for Toxicological Research
unknown
Research Areas
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Biography and Research Information
OverviewAI-generated summary
Tsung‐Jen Liao's research investigates the genetic and computational factors influencing drug-induced liver injury. His work includes analyzing the interaction of drug compounds with UDP-Glucuronosyltransferase (UGT) enzymes as a predictor of liver damage. Liao has explored the role of single-nucleotide polymorphisms and genetic variants, such as those in HLA class II genes and the GBP4 gene, in determining susceptibility and transplant-free survival in patients with acute liver failure. He also utilizes computational modeling and quantitative structure-activity relationship (QSAR) modeling to predict hepatotoxicity caused by drugs and chemicals. Additionally, his research extends to analyzing medical device reports to understand patient outcomes and adverse events, including sex-based differential effects. Liao has published nine papers and has a h-index of 3, with key collaborators including Minjun Chen, Kristin Ashby, R. E. Moore, and Bohu Pan, all from the National Center for Toxicological Research.
Metrics
- h-index: 3
- Publications: 9
- Citations: 27
Selected Publications
- Genetic Variants of <i>GBP4</i>: Reduced Risks for Drug‐Induced Acute Liver Failure in Non‐Finnish European Population (2025) DOI
- Drug interaction with UDP-Glucuronosyltransferase (UGT) enzymes is a predictor of drug-induced liver injury (2024) DOI
- Medical device report analyses from MAUDE: Device and patient outcomes, adverse events, and sex-based differential effects (2024) DOI
- QSAR modeling for predicting drug-induced liver injury (2023) DOI
- DILIrank dataset for QSAR modeling of drug-induced liver injury (2023) DOI
- Computational Modeling for the Prediction of Hepatotoxicity Caused by Drugs and Chemicals (2023) DOI
- Whole Exome Sequencing Reveals Genetic Variants in HLA Class II Genes Associated With Transplant-free Survival of Indeterminate Acute Liver Failure (2022) DOI
- Machine Learning to Identify Interaction of Single-Nucleotide Polymorphisms as a Risk Factor for Chronic Drug-Induced Liver Injury (2021) DOI
Collaborators
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